HGVS | Genome Assembly |
---|---|
NC_000012.12:g.93586007T= , CM000674.2:g.93586007T= | GRCh38 |
NC_000012.11:g.93979783T= , CM000674.1:g.93979783T= | GRCh37 |
NC_000012.10:g.92503914T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
XM_005269213.3:c.*248T= | XP_005269270.2:n.*248T= | |
XM_006719673.1:c.*248T= | XP_006719736.1:n.*248T= | |
XM_006719674.1:c.*248T= | XP_006719737.1:n.*248T= | |
XM_011538929.1:c.*248T= | XP_011537231.1:n.*248T= | |
XM_011538930.1:c.*248T= | XP_011537232.1:n.*248T= | |
XM_011538931.1:c.*248T= | XP_011537233.1:n.*248T= | |
XM_011538932.1:c.*248T= | XP_011537234.1:n.*248T= | |
XM_011538933.1:c.*248T= | XP_011537235.1:n.*248T= | |
XM_011538934.1:c.*248T= | XP_011537236.1:n.*248T= | |
XM_011538935.1:c.591+10834T= | XP_011537237.1:n.591+10834T= | |
XR_944810.1:n.1592T= |